Evidence map›Paper›PMID 30451486›Full record

ArticleACS applied materials & interfaces2018

An Immuno-Biochip Selectively Captures Tumor-Derived Exosomes and Detects Exosomal RNAs for Cancer Diagnosis.

Yunchen Yang, Eric Kannisto, Guan Yu, Mary E Reid, Santosh K Patnaik, Yun Wu

Open access · greenAbstract read
In one paragraph

Article in ACS applied materials & interfaces, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 107 citations in OpenAlex.

  1. Exosomes in pathogenesis, diagnosis, and therapy of ischemic stroke.Frontiers in bioengineering and biotechnology · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Yunchen YangDepartment of Biomedical Engineering , University at Buffalo, The State University of New York , 332 Bonner Hall , Buffalo , New York 14260 , United States.
Eric Kannisto
Guan YuDepartment of Biostatistics , University at Buffalo, The State University of New York , 710 Kimball Tower , Buffalo , New York 14214 , United States.
Mary E Reid
Santosh K Patnaik
Yun WuDepartment of Biomedical Engineering , University at Buffalo, The State University of New York , 332 Bonner Hall , Buffalo , New York 14260 , United States.ORCID http://orcid.org/0000-0002-6926-777X
Roswell Park Comprehensive Cancer Center · USUniversity at Buffalo, State University of New York · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
University of Buffalo Clinical and Translational Science Institute - Supplement SchulyerUL1TR001412 · NCATS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI MURPHY, TIMOTHY F · 2015 to 2024
$33.8M
Noninvasive detection of circulating RNAs for lung cancer early detection and prognosisR33CA191245 · NCI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI WU, YUN · 2015 to 2018
$1.3M
MicroRNA profiling to predict recurrence after resection of early lung cancerK23CA149076 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI YENDAMURI, SAIKRISHNA · 2011 to 2016
$937k
NCATS NIH HHS UL1 TR001412NCI NIH HHS K23 CA149076NCI NIH HHS P30 CA016056NCI NIH HHS R33 CA191245
6 · The paper itself

Abstract

Tumor-derived exosomes (TEXs) play instrumental roles in tumor growth, angiogenesis, immune modulation, metastasis, and drug resistance. TEX RNAs are a new class of noninvasive biomarkers for cancer. Neither current techniques, such as quantitative reverse transcription polymerase chain reaction (qRT-PCR) and next-generation sequencing, nor new ones, such as electrochemical or surface plasmon resonance-based biosensors, are able to selectively capture and separate TEXs from normal cell-derived exosomes, making TEX RNAs potentially less sensitive biomarkers. We developed an immuno-biochip that selectively captures TEXs using antibodies against tumor-associated proteins and quantifies in situ TEX RNAs using cationic lipoplexes containing molecular beacons. We used the immuno-biochip to measure the expression of miR-21 microRNA and TTF-1 mRNA in EGFR- or PD-L1-bearing exosomes from human sera and achieved absolute sensitivity and specificity in distinguishing normal controls from non-small cell lung cancer patients. Our results demonstrated that the effective separation of TEXs from other exosomes greatly improved the detection sensitivity and specificity. Compared with the traditional immunomagnetic separation-RNA isolation-qRT-PCR workflow, the immuno-biochip showed superior lung cancer diagnostic performance, consumed less samples (∼30 μL), and shortened assay time from ∼24 to 4 h.

Indexed as

Biomarkers, TumorCarcinoma, Non-Small-Cell LungCell-Free Nucleic AcidsExosomesLung NeoplasmsMicroarray AnalysisRNA, NeoplasmA549 CellsAntibodies, NeoplasmFemaleHumansMaleNeoplasm ProteinsReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionAntibodies, NeoplasmBiomarkers, TumorCell-Free Nucleic AcidsNeoplasm ProteinsRNA, Neoplasmcancer diagnosiscirculating biomarkerexosomesliquid biopsymicroRNA

Identifiers

PMID30451486
PMCPMC8628516
OpenAlexW2900860187

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.